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Fig. 1–3 in A new species of Eimeria Schneider, 1875 from the Serra dos Órgãos National Park, Rio de Janeiro, Brazil, with notes on its endogenous development in the montane grass mouse, Akodon montensis Thomas, 1913 (Rodentia: Sigmodontinae)
Fig. 1–3 Nomarski interference-contrast photomicrographs of Eimeria akodonensis n. sp. from the montane grass mouse, Akodon montensis. Presence of oocyst residuum (Or) and highly refractile polar granule (Pg); Sporocyst residuum (Sr); wall (Ow); Stieda body (Sb); sporozoite (Sp). Scale bar = 10 μm
Fig. 5–12 in A new species of Eimeria Schneider, 1875 from the Serra dos Órgãos National Park, Rio de Janeiro, Brazil, with notes on its endogenous development in the montane grass mouse, Akodon montensis Thomas, 1913 (Rodentia: Sigmodontinae)
Fig. 5–12 Light micrographs of the endogenous stages of Eimeria akodonensis n. sp. observed in the lamina propria of the small intestine of Akodon montensis, showing the microgamonts (Mi) and the parasitophorous vacuole in the host cell (Vp); microgametes (Mi); macrogamonts (Ma); nucleus (N) and the zygote (Zy) with wallforming bodies arranged around its periphery (Ow); oocyst (Oo). Scale bar = 10 μm
Fig. 4 in A new species of Eimeria Schneider, 1875 from the Serra dos Órgãos National Park, Rio de Janeiro, Brazil, with notes on its endogenous development in the montane grass mouse, Akodon montensis Thomas, 1913 (Rodentia: Sigmodontinae)
Fig. 4 Composite line drawing of the sporulated oocyst of Eimeria akodonensis n. sp. Scale bar = 10 μm
Figure 5 in Effect of environmental factors on the germination and emergence of drunken horse grass (Achnotherum inebrions)
Figure 5. Effect of osmotic potential on the germination of Achnotherum inebrions seeds at 25 C. Vertical bars represent the standard error of the mean, and a logistic sigmoidal regression model is fit to the data.
Figure 6 in Effect of environmental factors on the germination and emergence of drunken horse grass (Achnotherum inebrions)
Figure 6. Germination of Achnotherum inebrions seeds at low osmotic potential. The vertical bars represent the standard error of the mean. Bars with the same letters indicate that there are no significant differences in the mean values by Fisher's protected LSD test (P ≤ 0.05).
Figure 7 in Effect of environmental factors on the germination and emergence of drunken horse grass (Achnotherum inebrions)
Figure 7. Effect of burial depth on the emergence of A. inebrions seeds at 25 C. Vertical bars represent the standard error of the mean,and a logistic sigmoidal regression model is fit to the data.
Figure 4 in Effect of environmental factors on the germination and emergence of drunken horse grass (Achnotherum inebrions)
Figure 4. Effect of buffered pH solutions on the germination of Achnotherum inebrions seeds at 25 C. The vertical bars represent the standard error of the mean. Bars with the same letters indicate that there are no significant differences in the mean values by Fisher's protected LSD test (P ≤ 0.05).
Figure 3 in Effect of environmental factors on the germination and emergence of drunken horse grass (Achnotherum inebrions)
Figure 3. Effects of different photoperiods on the germination of Achnotherum inebrions seeds under 25 C culture conditions. Bars with the same letters indicate that there are no significant differences in the mean values by Fisher's protected LSD test (P ≤ 0.05).
Figure 2 in Effect of environmental factors on the germination and emergence of drunken horse grass (Achnotherum inebrions)
Figure 2. Effect of rewarming on the germination of Achnotherum inebrions seeds at 30/20 C. Rewarming refers to the transfer of ungerminated seeds kept under a constant temperature of 10, 35, or 40 C to a growth chamber set at the optimal temperature, 25 C (CK). The vertical bars represent the standard error of the mean. Bars with
Figure 1 in Effect of environmental factors on the germination and emergence of drunken horse grass (Achnotherum inebrions)
Figure 1. Effect of rewarming on the germination of Achnotherum inebrions seeds at 25 C. Rewarming refers to the transfer of ungerminated seeds kept under a constant temperature of 10, 35, or 40 C to a growth chamber set at the optimal temperature, 25 C (CK). The vertical bars represent the standard error of the mean. Bars with the same
Figure 2 in Assessing grass carp (Ctenopharyngodon idella) occupancy and detection probability within Lake Erie from environmental DNA
Figure 2. Mean posterior estimates of the probability of capturing grass carp eDNA from a site in a sample among sites (θ) from the model with the lowest WAIC score [ψ(Site)Θ(Site)p(.)]. Error bars represent 95% credible intervals. DR = Detroit River, HP = Hot Ponds, MB = Maumee Bay. All sites are located in western Lake Erie.
Figure 1 in Assessing grass carp (Ctenopharyngodon idella) occupancy and detection probability within Lake Erie from environmental DNA
Figure 1. Map denoting all monthly grass carp eDNA sampling events in 2018 (A–C) and 2019 (D–F) aggregated at each sampling location (Hot Ponds, Detroit River, and North Maumee Bay) and acoustic receiver locations (grey circles) in the western basin of Lake Erie. Positive and negative eDNA detections, defined as at least one positive qPCR detection on one replicate among all markers (GCTM10, GCTM22, GCTM32) are denoted by orange crosses and pink triangles, respectively. The 3 grass carp captured from conventional gear (total sampling events = 451) in the Detroit River (October 2018), Hot Pond (July 2019) and North Maumee Bay (July 2019) are denoted by a yellow hexagon.
Figure 2 in Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 2: Grass species
Figure 2. Cumulative percent shatter over four time periods (maturity, maturity + 2 wk, maturity + 3 wk, maturity + 4 wk) for each species. The darker the bar, the greater percent of sampled site-years that corresponded to the percent shatter value. This normalizes across species with different sampling efforts. Species sampled in just a single site-year are indicated by a single black square, which represents 100% of the sampling effort. Species are denoted by their EPPO codes
Figure 3 in Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 2: Grass species
Figure 3. Cumulative percent seed shatter for all species from planting date to soybean physiological maturity (black vertical line) across the participating states in 2016 and 2017.
Figure 1. Heat map indicating the cumulative percent seed shatter across the participating states for a in Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 2: Grass species
Figure 1. Heat map indicating the cumulative percent seed shatter across the participating states for a window starting from soybean physiological maturity to 4 wk past physiological maturity in 2016 and 2017. States were included in these maps only if they conducted sampling during the week indicated. (e.g., In 2017, Arkansas sampled on October 2, October 18, and November 3, none of which are within ±3 d of the October 10 maturity date or maturity +2 wk on October 24 in the state that year. Hence only data from maturity +3 wk are for Arkansas for 2017.)
Fig 1a in Efficacy of Doob grass, Cynodon dactylon against white spot syndrome virus in Penaeus monodon
Fig 1a: GCMS chromatogram of Cynodon dactylon extract showing fraction peaks at normal (300C) temperature. The peak in circle shows the original presence of ingredients in the C. dactylon before heating at higher temperature.
Fig. 8. Aculodes capillarisi n in New Species Of Aculodes (Acari: Eriophyoidea) From Grasses In Poland
Fig. 8. Aculodes capillarisi n. sp., nymph: D – dorsal aspect, DO – dorsal microtubercles, CG – coxigenital region
Fig. 5. Aculodes capillarisi n in New Species Of Aculodes (Acari: Eriophyoidea) From Grasses In Poland
Fig. 5. Aculodes capillarisi n. sp., female: D – dorsal aspect, em – empodium, IG – internal genitalia, DO – dorsal microtubercles
Fig. 1. Aculodes calamaabditus n in New Species Of Aculodes (Acari: Eriophyoidea) From Grasses In Poland
Fig. 1. Aculodes calamaabditus n. sp., female: D – dorsal aspect, IG – internal genitalia, DO – dorsal microtubercles, L1, L2 – leg I and II
Fig. 3. Aculodes calamaabditus n in New Species Of Aculodes (Acari: Eriophyoidea) From Grasses In Poland
Fig. 3. Aculodes calamaabditus n. sp., male: PS – prodorsal shield, CGM – coxigenital region, DO – dorsal microtubercles
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.